Evidence map›Paper›PMID 28123873›Full record

ArticleOncoimmunology

Rapid tumor regression in an Asian lung cancer patient following personalized neo-epitope peptide vaccination.

Fenge Li, Caixia Chen, Tao Ju, Junqin Gao, Jun Yan, Peng Wang, Qiang Xu, Patrick Hwu, Xueming Du, Gregory Lizée

Open access · goldAbstract read
In one paragraph

Article in Oncoimmunology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.6field-weighted citation impact, top 17% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

22 citing papers in PubMed, 29 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Tumor-Derived Antigenic Peptides as Potential Cancer Vaccines.International journal of molecular sciences · 2024
    Review
  6. Review
  7. Review
  8. Review
  9. Evolution of CD8Cells · 2021
    Review
  10. Article
  11. Review
  12. HLA Class I Binding of Mutant EGFR Peptides in NSCLC Is Associated With Improved Survival.Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer · 2021
    Article
  13. Review
  14. Divergent Peptide Presentations of HLA-AFrontiers in immunology · 2019
    Article
  15. Review
  16. Article
  17. Review
  18. Article
  19. Review
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 6 institutions in 2 countries.

Fenge LiDepartment of Gynecology, Tianjin First Center Hospital, Tianjin, China; Tianjin HengJia Biotechnology Development Co., Ltd, Tianjin, China.
Caixia ChenDepartment of Oncology, Tianjin Beichen Hospital , Tianjin, China.
Tao JuDepartment of Oncology, Tianjin Beichen Hospital , Tianjin, China.
Junqin GaoPathology Department, Tianjin Beichen Hospital , Tianjin, China.
Jun YanPathology Department, Tianjin First Center Hospital , Tianjin, China.
Peng WangRegenerative Medicine Center, Third Central Hospital , Tianjin, China.
Qiang XuGenomiCare Biotechnology Co. Ltd ., Shanghai, China.
Patrick HwuDepartment of Melanoma Medical Oncology, University of Texas M.D. Anderson Cancer Center , Houston, TX, USA.
Xueming DuDepartment of Oncology, Tianjin Beichen Hospital , Tianjin, China.
Gregory LizéeDepartment of Melanoma Medical Oncology, University of Texas M.D. Anderson Cancer Center, Houston, TX, USA; Department of Immunology, University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Tianjin Beichen Hospital · CNThe University of Texas MD Anderson Cancer Center · USGenomiCare (China) · CNTianjin First Center Hospital · CNTianjin Medical University · CNTianjin Third Central Hospital · CN

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
NCI NIH HHS P30 CA016672
6 · The paper itself

Abstract

Personalized immunotherapy targeting tumor-specific mutations represents a highly promising approach to cancer treatment. Here, we describe an Asian lung squamous cell carcinoma patient demonstrating frank disease progression following chemotherapy and EGFR inhibitor treatment. Based on tumor mutational profiling and HLA typing, a saline-based multi-epitope peptide vaccine was designed and administered along with topical imiquimod as an adjuvant. Weekly neo-epitope peptide vaccination was followed by a rapid and dramatic regression of multiple lung tumor nodules, while a much larger liver metastasis remained refractory to treatment. Peripheral blood immune monitoring showed that specific cytotoxic T lymphocytes (CTLs) were induced primarily against peptide targets encompassing the widely shared EGFR L858R mutation, particularly one restricted to HLA-A*3101. Immunological targeting of this driver mutation may be of particular benefit to Asian lung cancer patients due to its relatively high prevalence within this patient population.

Indexed as

Cancer vaccinecytotoxic T cellsEGFR L858R mutationepidermal growth factor receptorlung cancerneo-epitopepersonalized immunotherapy

Identifiers

PMID28123873
PMCPMC5214696
OpenAlexW2528582910

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.